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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to submit a proposal to the Defence and Security Accelerator
Make building control applications to any local authority in England, Wales or Northern Ireland.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Submit new evidence if your asylum application has been refused and you have no more right to appeal - called ‘further submission’
What detailed information you need to send to HMRC to support your Research and Development (R&D) tax relief claim, and when and how to submit it.
How to apply for marketing authorisation via this new procedure.
Find out how to submit your research to Athena, Dstl's central repository of MOD-sponsored scientific and technical research reports.
Guidance for local authorities, port health authorities and food traders on how to submit a sample for referee analysis.
SLC is reminding new full time undergraduate students in England to apply for their student finance now.
Login or register to the DASA online submission service
Instructions on how members of the public can submit their submissions to support the work of the team of experts leading the review.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
Use this service to submit a mandatory occurrence notice and report for higher-risk buildings, including high-rise residential buildings, to the BSR.
How to submit an application, data package and company responses for proposed or existing authorisations in the UK.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Form (H3) for staphylococcus and streptococcus multiple isolates.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Sets out process and expectations on pre-application discussions.
Webinars for pharmaceutical companies, clinical trial sponsors, e-cigarette producers and brokers of medicinal products
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